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Dag E Undlien

Showing results (21-30 of 44) with videos related to

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Annals of the Rheumatic Diseases|September 8, 2009
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritisBeate Skinningsrud, Benedicte A Lie, Eystein S Husebye, et al.
Journal of Translational Autoimmunity|August 4, 2020
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's diseaseSigrid Aslaksen, Anette B Wolff, Magnus D Vigeland, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2011
Multiple loci in the HLA complex are associated with Addison's diseaseBeate Skinningsrud, Benedicte A Lie, Ewa Lavant, et al.
Frontiers in Endocrinology|October 16, 2019
Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's DiseaseSigrid Aslaksen, Paal Methlie, Magnus D Vigeland, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|December 1, 2012
Pet keeping and tobacco exposure influence CD14 methylation in childhoodMonica Cheng Munthe-Kaas, Randi J Bertelsen, Tale Maehre Torjussen, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regionsKaja K Selmer, Gregor D Gilfillan, Petter Strømme, et al.
The Journal of Clinical Endocrinology and Metabolism|October 28, 2009
Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registryMartina M Erichsen, Kristian Løvås, Beate Skinningsrud, et al.
The Journal of Allergy and Clinical Immunology|August 19, 2004
CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigmMonica Cheng Munthe-Kaas, Kai Håkon Carlsen, Peter J Helms, et al.
Human Immunology|September 18, 2007
Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravisMarte K Viken, Hege Dahlen Sollid, Geir Joner, et al.
Diabetes|January 15, 2008
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetesAnders Molven, Monika Ringdal, Anita M Nordbø, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Annals of the Rheumatic Diseases|September 8, 2009
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritisBeate Skinningsrud, Benedicte A Lie, Eystein S Husebye, et al.
Journal of Translational Autoimmunity|August 4, 2020
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's diseaseSigrid Aslaksen, Anette B Wolff, Magnus D Vigeland, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2011
Multiple loci in the HLA complex are associated with Addison's diseaseBeate Skinningsrud, Benedicte A Lie, Ewa Lavant, et al.
Frontiers in Endocrinology|October 16, 2019
Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's DiseaseSigrid Aslaksen, Paal Methlie, Magnus D Vigeland, et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|December 1, 2012
Pet keeping and tobacco exposure influence CD14 methylation in childhoodMonica Cheng Munthe-Kaas, Randi J Bertelsen, Tale Maehre Torjussen, et al.
European Journal of Human Genetics : EJHG|June 30, 2011
A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regionsKaja K Selmer, Gregor D Gilfillan, Petter Strømme, et al.
The Journal of Clinical Endocrinology and Metabolism|October 28, 2009
Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registryMartina M Erichsen, Kristian Løvås, Beate Skinningsrud, et al.
The Journal of Allergy and Clinical Immunology|August 19, 2004
CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigmMonica Cheng Munthe-Kaas, Kai Håkon Carlsen, Peter J Helms, et al.
Human Immunology|September 18, 2007
Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravisMarte K Viken, Hege Dahlen Sollid, Geir Joner, et al.
Diabetes|January 15, 2008
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetesAnders Molven, Monika Ringdal, Anita M Nordbø, et al.
Pageof 5